DeRoyal is recalling certain Children's Laptracepack surgical packs due to a Stryker SafeAir Smoke Evacuation Pencil activating without manual input when plugged in or remaining active after button release.
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source or remains active after buttons are released.
DeRoyal is recalling specific lots of Children's Laptracepack surgical packs because a Stryker SafeAir Smoke Evacuation Pencil inside can activate without manual input or stay active after buttons are released. This could lead to unintended smoke evacuation in medical settings.
The Stryker SafeAir Smoke Evacuation Pencil inside the pack can activate without manual input when plugged into a power source or remain active after buttons are released. This could cause unintended smoke evacuation during medical procedures, potentially disrupting surgery or causing safety issues.
Healthcare providers using the recalled Children's Laptracepack surgical packs are most at risk. The product is used in medical settings where unintended activation could disrupt procedures.
Check for the lot number 59244907 with expiration date 10/1/2025 on the DeRoyal Children's Laptracepack surgical packs. The product is sold in cases with UDI/DI numbers 00749756913393 (each) and 50749756913398 (case).
Verify the lot number 59244907 with expiration date 10/1/2025 on the DeRoyal Children's Laptracepack surgical packs.
DeRoyal is recalling certain lots of Children's Laptracepack surgical packs because a Stryker SafeAir Smoke Evacuation Pencil inside can activate without manual input when plugged in or remain active after buttons are released.
The official recall notice does not specify a remedy or action steps beyond checking product details for the recalled lot number.
The recall notice describes the hazard as unintended activation of the pencil, but does not mention specific injury risks or mechanisms.
We’ve drafted a message you can send DeRoyal to request your refund or repair — edit it as you like.
Subject: Recall Z-0309-2025 — DeRoyal DeRoyal Hello, I own a DeRoyal that is covered by recall Z-0309-2025 from DeRoyal. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
